ClinVar Miner

List of variants reported as likely benign for Darier disease

Included ClinVar conditions (1):
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Total variants: 13
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HGVS dbSNP
NM_170665.4(ATP2A2):c.*3837C>T rs769621334
NM_170665.4(ATP2A2):c.1122T>C (p.Gly374=) rs772617747
NM_170665.4(ATP2A2):c.136+11C>T rs769052817
NM_170665.4(ATP2A2):c.1569G>A (p.Arg523=)
NM_170665.4(ATP2A2):c.1627A>G (p.Lys543Glu)
NM_170665.4(ATP2A2):c.1758T>C (p.Tyr586=) rs145018250
NM_170665.4(ATP2A2):c.1983C>T (p.Asn661=) rs755494363
NM_170665.4(ATP2A2):c.2059G>A (p.Val687Ile)
NM_170665.4(ATP2A2):c.2295G>A (p.Ser765=)
NM_170665.4(ATP2A2):c.2318+3A>G
NM_170665.4(ATP2A2):c.2556A>C (p.Ala852=) rs201414100
NM_170665.4(ATP2A2):c.2860-10TG[2] rs372303998
NM_170665.4(ATP2A2):c.2945C>T (p.Thr982Met) rs149024535

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